Evidence map›Paper›PMID 38288966›Full record

ArticleOphthalmic genetics2024

A proposal for an updated staging system for LCHADD retinopathy.

Nida Wongchaisuwat, Melanie B Gillingham, Paul Yang, Lesley Everett, Ashley Gregor, Cary O Harding, Jose Alain Sahel, Ken K Nischal, Hannah L Scanga, Danielle Black and 3 more

Abstract read
In one paragraph

Article in Ophthalmic genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Nida WongchaisuwatCasey Eye Institute, Department of Ophthalmology, Oregon Health & Science University, Portland, Oregon, USA.
Melanie B GillinghamDepartment of Molecular and Medical Genetics, Oregon Health and Science University, Portland, Oregon, USA.
Paul YangCasey Eye Institute, Department of Ophthalmology, Oregon Health & Science University, Portland, Oregon, USA.
Lesley EverettCasey Eye Institute, Department of Ophthalmology, Oregon Health & Science University, Portland, Oregon, USA.
Ashley GregorDepartment of Molecular and Medical Genetics, Oregon Health and Science University, Portland, Oregon, USA.
Cary O HardingDepartment of Molecular and Medical Genetics, Oregon Health and Science University, Portland, Oregon, USA.
Jose Alain SahelDepartment of Ophthalmology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
Ken K NischalDepartment of Ophthalmology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.
Hannah L ScangaDepartment of Ophthalmology, University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, USA.ORCID 0000-0002-4004-3959
Danielle BlackDivision of Genetic and Genomic Medicine, University of Pittsburgh Medical Center Children's Hospital, Pittsburgh, Pennsylvania, USA.
Jerry VockleyDivision of Genetic and Genomic Medicine, University of Pittsburgh Medical Center Children's Hospital, Pittsburgh, Pennsylvania, USA.
Georgianne ArnoldDivision of Genetic and Genomic Medicine, University of Pittsburgh Medical Center Children's Hospital, Pittsburgh, Pennsylvania, USA.
Mark E PennesiCasey Eye Institute, Department of Ophthalmology, Oregon Health & Science University, Portland, Oregon, USA.

Funding

The Natural History of LCHAD RetinopathyR01HD095968 · NICHD · OREGON HEALTH & SCIENCE UNIVERSITY · PI GILLINGHAM, MELANIE B · 2019 to 2024
$2.7M
NICHD NIH HHS R01 HD095968
6 · The paper itself

Abstract

objectiveTo develop an updated staging system for long-chain 3-hydroxyacyl coenzyme A dehydrogenase deficiency (LCHADD) chorioretinopathy based on contemporary multimodal imaging and electrophysiology.

methodsWe evaluated forty cases of patients with genetically confirmed LCHADD or trifunctional protein deficiency (TFPD) enrolled in a prospective natural history study. Wide-field fundus photographs, fundus autofluorescence (FAF), optical coherence tomography (OCT), and full-field electroretinogram (ffERG) were reviewed and graded for severity.

resultsTwo independent experts first graded fundus photos and electrophysiology to classify the stage of chorioretinopathy based upon an existing published system. With newer imaging modalities and improved electrophysiology, many patients did not fit cleanly into a single traditional staging group. Therefore, we developed a novel staging system that better delineated the progression of LCHADD retinopathy. We maintained the four previous delineated stages but created substages A and B in stages 2 to 3 to achieve better differentiation. DISCUSSION: Previous staging systems of LCHADD chorioretinopathy relied on only on the assessment of standard 30 to 45-degree fundus photographs, visual acuity, fluorescein angiography (FA), and ffERG. Advances in recordings of ffERG and multimodal imaging with wider fields of view, allow better assessment of retinal changes. Following these advanced assessments, seven patients did not fit neatly into the original classification system and were therefore recategorized under the new proposed system.

conclusionThe new proposed staging system improves the classification of LCHADD chorioretinopathy, with the potential to lead to a deeper understanding of the disease's progression and serve as a more reliable reference point for future therapeutic research.

Indexed as

CardiomyopathiesChoroid DiseasesLipid Metabolism, Inborn ErrorsMitochondrial MyopathiesNervous System DiseasesRetinal DiseasesRhabdomyolysisFluorescein AngiographyHumansMitochondrial Trifunctional ProteinProspective StudiesRetinaTomography, Optical CoherenceMitochondrial Trifunctional ProteinchorioretinopathyLCHADDLCHAD deficiencystaging

Identifiers

PMID38288966
PMCPMC11010772

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.